Iron compounds catalyze the oxidation of 10-formyl-5,6,7,8 tetrahydrofolic acid to 10-formyl-7,8 dihydrofolic acid

We have previously demonstrated that 10-formyl-7,8-dihydrofolic acid (10-HCO-H 2folate) is a better substrate for mammalian aminoimidazolecarboxamide ribotide transformylase (EC 2.1.2.3) than is 10-formyl-5,6,7,8-tetrahydrofolic acid (10-HCO-H 4folate) (J.E. Baggott, G.L. Johanning, K.E. Branham, C....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of inorganic biochemistry 1998-09, Vol.71 (3), p.181-187
Hauptverfasser: Baggott, Joseph E, B. Robinson, Constance, Eto, Isao, Johanning, Gary L, Cornwell, Phillip E
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:We have previously demonstrated that 10-formyl-7,8-dihydrofolic acid (10-HCO-H 2folate) is a better substrate for mammalian aminoimidazolecarboxamide ribotide transformylase (EC 2.1.2.3) than is 10-formyl-5,6,7,8-tetrahydrofolic acid (10-HCO-H 4folate) (J.E. Baggott, G.L. Johanning, K.E. Branham, C.W. Prince, S.L. Morgan, I. Eto, W.H. Vaughn, Biochem. J. 308, 1995, 1031–1036). Therefore, the possible metabolism of 10-HCO-H 4folate to 10-HCO-H 2folate was investigated. A spectrophotometric assay for the oxidation of 10-HCO-H 4folate to 10-HCO-H 2folate which measures the disappearance of reactant (decrease in absorbance at 356 nm after acidification of aliquots of the reaction solution), is used to demonstrate that iron compounds catalyze the oxidation of 10-HCO-H 4folate to 10-HCO-H 2folate in the presence and absence of ascorbate. Chromatographic separation of the 10-HCO-H 2folate product from the reaction mixture, its UV spectra, a microbiological assay and an enzymatic assay established that the iron-catalyzed oxidation product of 10-HCO-H 4folate was 10-HCO-H 2folate; without substantial side reactions. The inhibition of this iron-catalyzed oxidation by deferoxamine, apotransferrin and mannitol and the stimulation by citrate and EDTA indicated a mechanism involving a reaction of 10-HCO-H 4folate with hydroxyl radicals ( •OH) generated by Fenton chemistry. The presence of “free iron” (e.g. Fe 3+ citrate) in bile, cerebrospinal fluid and intracellularly suggest that this oxidation could occur in vivo and that 10-HCO-H 4folate may be a •OH scavenger.
ISSN:0162-0134
1873-3344
DOI:10.1016/S0162-0134(98)10052-1